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Multicenter Typing Comparison of Sporadic and OutbreakClostridium difficileIsolates from Geographically Diverse Hospitals
Author(s) -
Matthew H. Samore,
George Killgore,
Stuart Johnson,
Richard Goodman,
Janet K. Shim,
Lata Venkataraman,
Susan P. Sambol,
Paola C. DeGirolami,
Fred C. Tenover,
Robert D. Arbeit,
Dale N. Gerding
Publication year - 1997
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/514117
Subject(s) - pulsed field gel electrophoresis , typing , clostridium difficile , outbreak , microbiology and biotechnology , diarrhea , polymerase chain reaction , virology , biology , infection control , medicine , genotype , genetics , gene , antibiotics , pathology
In a collaborative study by three laboratories, arbitrarily primed polymerase chain reaction (AP-PCR), HindIII restriction enzyme analysis (REA), and pulsed-field gel electrophoresis (PFGE) using SmaI were compared for typing of Clostridium difficile. The study included 30 isolates from nosocomial outbreaks in six geographically disparate hospitals and 15 isolates from sporadic cases of C. difficile diarrhea. REA distinguished a total of 23 types representing 10 groups; AP-PCR performed at Deaconess Hospital resolved 19 types; AP-PCR performed at the Centers for Disease Control resolved 15 types. Thirty isolates exhibited degradation of larger sized fragments during processing and therefore were nontypeable by PFGE; among the remaining 15 isolates, PFGE resolved 11 types. Outbreak isolates in five different hospitals represented REA group J and constituted a single AP-PCR strain. In summary, nosocomial outbreaks of C. difficile diarrhea in five hospitals were associated with a single genetic lineage as resolved by multiple strain typing systems.

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